rs3824067
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3824067(A;A) |
| Make rs3824067(A;T) |
| Make rs3824067(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 155461246 |
| Gene | EN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3824067 |
| dbSNP (classic) | rs3824067 |
| ClinGen | rs3824067 |
| ebi | rs3824067 |
| HLI | rs3824067 |
| Exac | rs3824067 |
| Gnomad | rs3824067 |
| Varsome | rs3824067 |
| LitVar | rs3824067 |
| Map | rs3824067 |
| PheGenI | rs3824067 |
| Biobank | rs3824067 |
| 1000 genomes | rs3824067 |
| hgdp | rs3824067 |
| ensembl | rs3824067 |
| geneview | rs3824067 |
| scholar | rs3824067 |
| rs3824067 | |
| pharmgkb | rs3824067 |
| gwascentral | rs3824067 |
| openSNP | rs3824067 |
| 23andMe | rs3824067 |
| SNPshot | rs3824067 |
| SNPdbe | rs3824067 |
| MSV3d | rs3824067 |
| GWAS Ctlg | rs3824067 |
| GMAF | 0.1524 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
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[PMID 20523082] Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population
[PMID 16252243
] Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.
